Industry News 行业新闻 – Page 2

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IATA DGR 67 in Force: Understanding the 30% Lithium Battery Charge Limit IATA DGR 67

Effective January 1, 2026, the International Air Transport Association (IATA) Dangerous Goods Regulations Edition 67 (DGR 67) came into force. According to a technical analysis published by Jauch Quarz on January 15, 2026, this update upgrades the lithium battery air transport state-of-charge (SoC) requirement from a previous recommendation of no more than 30% to a mandatory enforcement standard. This change directly affects cross-border transport of smart devices containing lithium batteries.

Key Regulatory Changes

Mandatory SoC ≤30%: Lithium-ion batteries packed with equipment (UN3481) and those shipped separately (UN3480) must not exceed 30% state of charge during air transport. Previously a recommendation, this threshold is now a mandatory requirement. Non-compliant shipments will be rejected at airports, potentially causing logistics delays and additional costs.
Installed battery exception: Only batteries already installed inside equipment (UN3482) may be transported at a state of charge above 30%. This means products shipped with batteries pre-installed in the device enjoy greater transport flexibility compared to products where batteries are packaged separately.
UN38.3 Rev.8 simultaneously mandatory: The eighth revision (Rev.8) of the UN38.3 testing standard is now globally mandatory, and previous edition test reports are no longer valid. The new revision adds combined temperature cycling and mechanical shock testing, raising the safety verification threshold. Suppliers holding older edition reports must resubmit for testing, which may affect supply continuity during the transition period.

Impact on Cross-Border E-Commerce and Consumers

This regulation affects cross-border transport of smart devices containing lithium batteries in several ways:

Shipping timelines: Manufacturers and logistics providers must discharge batteries to below 30% before shipment and ensure possession of Rev.8 UN38.3 test reports. Non-compliant shipments may be rejected at airports or held by customs. Consumers may experience slightly longer wait times after ordering, particularly during the initial transition period following implementation of the new rules.
Receiving experience: Consumers receiving devices with lithium batteries may need to charge them before first use, as batteries are controlled at low charge levels to comply with air transport requirements. This is normal behavior and does not indicate a product quality issue.
Rated energy tiers: Lithium-ion batteries with rated energy ≤100Wh may be transported via standard passenger aircraft channels; 100–160Wh requires written airline approval; above 160Wh is prohibited on passenger aircraft. Most smart home device batteries fall within these limits, but large energy storage devices or power tools may require special arrangements.

Smart devices containing lithium batteries shipped from this site strictly comply with IATA DGR 67 and related transport regulations. For delivery arrangements and shipping restrictions, please refer to our Shipping Policy. We commit to arranging shipment within 1–3 business days after order placement.

参考来源 / Sources

Jauch Quarz (citing IATA DGR 67 original text), 2026-01-15, UN 38.3 New Regulations for Air Transport of Lithium Batteries

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ISO/CIE 8995-1:2025: Circadian Lighting Enters International Standards ISO/CIE 8995-1:2025

On January 31, 2025, the updated ISO/CIE 8995-1:2025 international standard for indoor workplace lighting was officially published. This is the first international standard to incorporate quantified non-visual effects (circadian stimulation) into indoor lighting specifications. According to a technical analysis published by BrainLit on February 17, 2025, the standard introduces for the first time circadian lighting recommendations based on melanopic Equivalent Daylight Illuminance (m-EDI).

m-EDI Recommended Values Explained

The standard establishes the following m-EDI recommendations for different times of day:

Daytime: Minimum 250 lux m-EDI to maintain normal circadian signaling and alertness. Adequate daytime light signals help anchor the body’s biological clock, improving nighttime sleep quality.
Three hours before bedtime: Maximum 10 lux m-EDI to reduce suppression of melatonin secretion. Melatonin is a key hormone for natural sleep onset, and excessive blue light stimulation can delay its secretion peak.
During nighttime sleep: Maximum 1 lux m-EDI to minimize light disruption to sleep cycles. Even dim nightlight illumination, if its spectrum contains significant short-wavelength components, may affect the proportion of deep sleep.

m-EDI is a metric that measures the intensity of light stimulation on the human non-visual system, particularly the melanopsin-containing photoreceptors that regulate circadian rhythms. Unlike traditional illuminance (lux), it accounts for the influence of spectral composition on biological effects. Two lamps with identical traditional illuminance may have significantly different m-EDI values if their color temperatures differ.

Implications for Smart Lighting Selection

The publication of this standard provides an international reference benchmark for tunable color temperature smart lighting. When selecting products, consumers can consider:

Whether the product specifies m-EDI values or equivalent circadian lighting parameters, indicating that the manufacturer considered non-visual health factors in the design rather than focusing solely on traditional brightness metrics.
Whether the fixture supports automatic adjustment of color temperature and brightness by time of day, enabling circadian-friendly modes with high-illuminance cool white light during daytime and low-illuminance warm light at night. This automation capability is one of the core values distinguishing smart lighting from conventional fixtures.
Understanding the distinction between m-EDI and traditional illuminance: high traditional illuminance does not equal high circadian stimulation; spectral composition matters equally. When selecting products, consumers should look beyond lumen or lux ratings and also consider spectral characteristics.

Our smart lighting category (30 products) includes various tunable color temperature fixtures. Specific spectral parameters and circadian lighting features should be verified on the product detail pages. For inquiries, please visit Contact Us.

参考来源 / Sources

ISO / CIE (via BrainLit technical analysis), standard published 2025-01-31 / analysis 2025-02-17, A New Global Standard for Indoor Lighting: ISO 8995-1

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EU Standby Power Limits Take Effect: What It Means for Smart Appliances

European Commission Regulation (EU) 2023/826 took effect on May 9, 2025, establishing new upper limits on standby mode power consumption for electrical and electronic equipment. According to a press release from the European Commission Directorate-General for Energy dated May 8, 2025, the new regulation covers approximately 800 million products sold annually and is projected to save 4 TWh of electricity per year by 2030, translating to EUR 530 million in annual consumer savings.

Key Limits and Timelines

Off mode: Power consumption capped at 0.5W; further reduced to 0.3W starting May 9, 2027. This means devices that are fully switched off but still connected to mains power will have their energy draw strictly limited.
Networked standby mode: Upper limit set at 2–7W, with specific values depending on product category. Networked standby refers to the state where a device maintains a network connection to receive remote commands or updates, which is the most common low-power operating mode for smart home devices.
Newly covered categories: Wi-Fi routers, wireless speakers, electric standing desks, and motorized blinds, previously outside the scope of regulation, are now subject to the new requirements. These categories happen to be core components of the smart home ecosystem.

Impact on Smart Home Products

Smart home devices, due to their “always-on” nature, have long been a focus of energy efficiency concerns regarding standby power. The implementation of this regulation means:

Smart appliances, routers, speakers, and similar products exported to the EU market must meet the new standby power limits or cannot be sold within the EU. For cross-border e-commerce sellers targeting the European market, this represents a hard market access threshold.
For consumers, compliant products will consume less standby power in daily use, contributing to lower electricity costs over time. For a household with ten or more smart devices, saving several watts of standby power per device creates a cumulative effect that should not be overlooked.
Routers, as the central hub of home networks, have standby power performance that directly affects overall household energy consumption. Including Wi-Fi routers in the regulatory scope encourages manufacturers to optimize low-power designs while maintaining network availability.

Our smart appliances category (30 products), networking category (25 products), and smart speakers category (30 products) encompass a variety of product types. Energy efficiency parameters and applicable markets for each product should be verified on the product detail pages. Learn more at About Us.

参考来源 / Sources

European Commission Directorate-General for Energy, 2025-05-08, EU Consumers Save Energy: New Limits on Standby Modes

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FDA’s 2026 General Wellness Guidance: Where Wearables Cross the Line FDA 2026

On January 6, 2026, the U.S. FDA issued an updated “General Wellness: Policy for Low Risk Devices” guidance document, replacing the 2019 version. This guidance explicitly clarifies for the first time that wearable devices monitoring physiological parameters such as blood pressure, blood glucose, and blood oxygen may be exempt from medical device regulation under specific conditions. According to Troutman Pepper law firm’s analysis, this update responds to industry controversy following the FDA’s July 2025 warning letter to WHOOP, which determined that its “Blood Pressure Insights” feature constituted an unapproved medical device.

Exemption Conditions and Compliance Boundaries

According to the guidance, wearable devices must simultaneously meet the following conditions to qualify for the “general wellness” exemption:

Non-invasive sensing: Data collection methods must not penetrate the skin or enter the body. This means transmissive sensors such as fingertip pulse oximeters may not qualify for the exemption, while reflective optical sensors on the back of a watch may meet the criteria.
Claims limited to “general wellness” purposes: Marketing materials must not claim the ability to diagnose, treat, prevent, or mitigate any disease. Language should be confined to categories such as “healthy lifestyle support” or “promoting physical wellness awareness.” Even technically accurate descriptions may trigger regulatory scrutiny if they imply a disease association.
No disease association: Even if a product is technically capable of detecting a physiological abnormality, associating that abnormality with a specific disease may result in classification as a medical device. The WHOOP case serves as a typical cautionary example: although the product was positioned as a “health tracker,” the naming and marketing of its “Blood Pressure Insights” feature implied an association with hypertensive disease, leading the FDA to classify it as an unapproved medical device.

Reference Value for Consumers

This guidance provides consumers with a framework for evaluation: when a wearable device’s claimed functions extend beyond the “general wellness” scope into the realm of disease diagnosis or treatment, it should hold appropriate medical device authorization. If a product makes medical-related claims without such authorization, consumers should exercise caution. At the same time, data from compliant “general wellness” devices still holds reference value, though it should not be treated as a substitute for medical diagnosis.

Important Disclaimer: The Smart Blood Glucose Meter GL1, Smart Electronic Blood Pressure Monitor BM1, Smart Body Fat Scale B1, Smart Band H1, and Smart Band H2 sold on this site are not medical devices. They are not intended for diagnosis or treatment of any disease. Data collected by these products is provided solely for general wellness and lifestyle reference purposes. If you feel unwell, please consult a healthcare professional. Our products are positioned as healthy lifestyle support tools and do not constitute medical advice. For specific product information, please refer to the product detail pages. Compliance and safety details are available on our Product Compliance and Safety page.

参考来源 / Sources

U.S. FDA / Troutman Pepper Law Firm Analysis, 2026-01-06, FDA’s 2026 Guidance on General Wellness Devices

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FDA Warns on Unauthorized Blood Pressure Devices: What Consumers Should Check FDA

On September 16, 2025, the U.S. Food and Drug Administration (FDA) issued a safety communication warning consumers against using blood pressure measuring devices that have not been authorized by the FDA. The FDA explicitly stated that such devices, including blood pressure software features embedded in smartwatches and smart rings, have not undergone FDA review for safety and effectiveness. Inaccurate readings could lead users to delay seeking medical care, potentially resulting in serious consequences such as stroke or heart attack.

Key FDA Recommendations

In its communication, the FDA advises consumers to search for product code DXN in the 510(k) database to verify whether a specific blood pressure measuring device has received FDA authorization. Only devices that have passed 510(k) review and obtained authorization may legally be marketed in the United States as blood pressure measuring medical devices.

This communication was prompted by the growing number of consumer wearable devices on the market claiming blood pressure measurement capabilities, many of which have not gone through the medical device approval process. The FDA’s action aims to help consumers distinguish between “health monitoring features” and “medical diagnostic functions.” Importantly, the FDA’s warning targets devices that claim blood pressure measurement capability without authorization, not all wearable health products.

How Consumers Should Evaluate

Faced with a wide variety of blood pressure-related products, consumers can consider the following approach:

Distinguish intended use: If a product claims it can be used to diagnose, treat, or monitor conditions such as hypertension, it should have obtained FDA 510(k) authorization. Products making such claims without authorization carry compliance risks, and consumers should exercise caution.
Verify authorization status: Searching product code DXN in the FDA 510(k) database can confirm whether a specific device appears on the authorized list. This is a publicly accessible database that consumers can search independently.
Interpret health data rationally: Data provided by health monitoring devices that lack medical device authorization should serve only as lifestyle references and should not form the basis for medical decisions. Even if data shows abnormalities, confirmation through proper medical channels is recommended.

Important Disclaimer: The Smart Blood Glucose Meter GL1, Smart Electronic Blood Pressure Monitor BM1, Smart Body Fat Scale B1, Smart Band H1, and Smart Band H2 sold on this site are not medical devices. They are not intended for diagnosis or treatment of any disease. Data collected by these products is provided solely for general wellness and lifestyle reference purposes. If you feel unwell, please consult a healthcare professional. These products have not received FDA 510(k) authorization and must not be used as substitutes for professional medical equipment. For specific product information, please refer to the product detail pages. Compliance and safety details are available on our Product Compliance and Safety page.

参考来源 / Sources

U.S. Food and Drug Administration (FDA), 2025-09-16, Do Not Use Unauthorized Devices for Measuring Blood Pressure

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California’s New CCPA Rules: ADMT and Annual Security Audits

On July 24, 2025, the California Privacy Protection Agency (CPPA) formally adopted updated rules under the CCPA (California Consumer Privacy Act). These updates introduce two requirements with direct implications for the smart home industry: a definition and regulatory framework for Automated Decision-Making Technology (ADMT), and an obligation for businesses to conduct annual third-party cybersecurity audits. Related information was republished by the Shenzhen Municipal Bureau of Justice, and O’Melveny law firm published a compliance checklist on April 13, 2026, providing further interpretation.

Two Core New Requirements

Automated Decision-Making Technology (ADMT): The new rules provide the first explicit definition of ADMT and require businesses using high-risk automated decision systems to conduct impact assessments. For the smart home sector, this means that if a product uses algorithms to make decisions significantly affecting user rights (such as credit scoring or insurance pricing based on behavioral data), additional transparency and assessment obligations may apply. Simple automated on-off controls generally do not fall into the high-risk category, but scenarios involving personal profiling or differential pricing require careful evaluation.
Annual Cybersecurity Audits: Businesses must engage third parties to conduct cybersecurity audits annually and maintain risk assessment documentation on file. This requirement applies to various businesses that process personal information of California residents, including cross-border e-commerce platforms. Audit scope covers multiple dimensions including data access controls, encryption measures, and incident response procedures, aiming to ensure that businesses’ data protection practices align with their public commitments.

Additionally, as of March 2026, 20 U.S. states have enacted comprehensive privacy laws, reflecting an accelerating trend in data protection legislation across the country. For e-commerce businesses operating nationwide, compliance obligations are expanding from a single state to an increasingly complex overlay of multi-state requirements.

Significance for Smart Home Consumers

Strengthened privacy regulations represent a positive signal for consumers. When businesses are required to undergo annual security audits and impact assessments, it means user data is subject to stricter institutional safeguards during processing. When selecting smart home products, consumers can consider whether manufacturers publicly disclose their data handling practices and security audit status as one dimension of trustworthiness.

Our business is registered in Massachusetts, United States, and we are committed to complying with applicable privacy regulations, including the CCPA where it reaches our California customers. For details on our data handling practices, please refer to our Privacy Policy; for service terms, see our Terms of Service.

参考来源 / Sources

CPPA Official Rules (republished by Shenzhen Municipal Bureau of Justice), 2025-07-24, California Privacy Protection Agency CCPA Updated Rules
O’Melveny Law Firm Compliance Checklist, 2026-04-13

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Solar Camera Recall: A Hardware Safety Reminder for Home Security

In June 2026, the U.S. Consumer Product Safety Commission (CPSC) issued a recall notice announcing that Wyze Labs was recalling over 320,000 Solar Cam Pan security cameras. The recall was prompted by errors in the product’s assembly instructions, which could lead users to puncture the built-in lithium battery during installation, creating fire and burn hazards. Details are available on the official CPSC recall page.

Background and Details of the Recall

The recalled product is a solar-powered outdoor security camera with a built-in lithium battery designed to sustain operation during periods without sunlight. According to the CPSC announcement, the issue does not stem from a design defect in the battery itself, but rather from incorrect assembly instructions that could cause users to accidentally damage the battery enclosure during installation, potentially resulting in short circuits or thermal runaway.

This incident serves as a reminder that safety risks in home security products extend beyond software vulnerabilities or privacy concerns. Hardware-level design quality and documentation accuracy directly impact user safety. Lithium batteries, as high-energy-density storage components, can release significant heat in a short period once their physical enclosure is compromised, triggering an uncontrollable chain reaction.

Lessons for Consumers

While this recall targets a specific brand and model, the underlying issues offer broadly applicable guidance:

Monitor recall notices: After purchasing a security camera, periodically check recall announcements from the CPSC or relevant regulatory bodies in your region to confirm whether your device is among affected batches. Many consumers rarely proactively check for recall information after purchase, potentially missing critical safety notifications.
Follow installation instructions carefully: When installing devices containing lithium batteries, strictly adhere to the provided manual. If instructions appear unclear or inconsistent with the physical product, pause installation and contact the manufacturer. Never rely on guesswork for installation steps, especially those involving battery compartment access.
Evaluate safety comprehensively: When selecting security products, look beyond functional specifications such as resolution and night vision range. Also consider whether the product has passed relevant physical safety testing and certifications. Hardware safety is equally as important as data security and should not be overlooked.

Our smart security category (30 products) includes various cameras and doorbell products. For specific safety certification information and usage instructions, please refer to the product detail pages. For returns, please consult our Refund and Return Policy, which provides a 30-day return window.

参考来源 / Sources

U.S. Consumer Product Safety Commission (CPSC), 2026-06, Wyze Labs Recalls Solar Cam Pan Security Cameras

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China’s Mandatory E-Lock Standard: What Biometric Anti-Spoofing Rules Mean

China’s mandatory national standard GB 21556.2-2025, titled “Lock Safety Technical Specifications Part 2: Electronic Locks,” was published on September 29, 2024, and took effect on March 1, 2026. The standard was issued by the State Administration for Market Regulation and can be accessed through the National Standards Full Text Disclosure System. As smart door locks gain widespread adoption in the Chinese market, this standard establishes clear baseline requirements for biometric security in electronic locks.

Core Safety Requirements

According to the standard text, the new regulation sets explicit anti-spoofing technical requirements for biometric modules in electronic locks:

Facial recognition: Must employ 3D structured light or binocular infrared liveness detection technology. Two-dimensional planar recognition methods are prohibited. This requirement aims to prevent spoofing via photographs or video replays. In the past, some lower-priced products used only basic cameras for facial comparison, which could be bypassed with high-resolution photos or screen captures.
Fingerprint recognition: Must use semiconductor-based liveness detection and include defenses against AI-generated deepfake forgeries. Traditional optical fingerprint sensors, which struggle to distinguish real from fake fingerprints, no longer meet the standard. As generative AI technology advances, the barrier to fingerprint forgery has decreased, and the standard addresses this proactively.
Mechanical lock cylinder: Class C lock cylinders must resist technical picking attempts for no less than 15 minutes, establishing a baseline for physical security. Even when electronic systems fail, the mechanical lock cylinder must provide basic anti-pick protection.

Relevance for Consumers

As a mandatory national standard, electronic lock products sold in the Chinese market must comply with its requirements. Consumers can use this standard as a reference when evaluating the biometric security level of door locks:

When selecting a facial recognition lock, verify that the product description specifies “3D structured light” or “binocular infrared” liveness detection, rather than merely stating “facial recognition.” Vague descriptions may indicate the use of 2D methods that the standard has phased out.
When choosing a fingerprint lock, look for explicit mention of “semiconductor liveness detection” and avoid older models using only optical fingerprint sensors. Semiconductor sensors outperform traditional optical solutions in both anti-spoofing capability and recognition speed.
Understand the basic meaning of Class C lock cylinders as a reference point for mechanical security. The lock cylinder grade represents the last line of physical defense when an electronic lock loses power or malfunctions.

It is important to note that this standard represents Chinese domestic safety design requirements and does not indicate that any specific product has been certified to this standard. For specific specifications and compliance status of products in our smart locks category (30 products), please refer to the product detail pages. Learn more at About Us.

参考来源 / Sources

National Standards Full Text Disclosure System, published 2024-09-29 / effective 2026-03-01, GB 21556.2-2025 Lock Safety Technical Specifications

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Thread 1.4 Is Now the Only Certified Version, but Platform Support Lags Thread 1.4

Thread 1.4 was released in September 2024 and has been the sole version accepted for certification by the Thread Group since January 2026. Its core improvement is a cross-vendor credential sharing mechanism that allows border routers from different brands to join the same mesh network, theoretically eliminating the problem of devices operating in isolated sub-networks. For smart home devices that rely on low-power wireless mesh networking, the progress toward Thread unification directly affects the practical usability of multi-brand systems.

Standard Is Ready, but Platform Adoption Lags

However, the publication of the standard does not mean all platforms have upgraded simultaneously. According to The Verge, reporting on September 2, 2026, Apple only added Thread 1.4 support in the tvOS 26 beta, while Amazon and Google platforms remain on Thread 1.3. This means that even if consumers purchase Thread 1.4-certified devices, they may still be unable to achieve a unified cross-platform mesh network in practice.

The Verge’s report cites tvOS 26 beta code as evidence, lending high credibility to this finding. The current situation indicates that while the unified vision of Thread 1.4 is technically ready, commercial platform implementation still depends on software updates from each vendor. For consumers, this means that the “Thread certified” label alone does not guarantee actual cross-brand interoperability; the firmware version of the platform being used must also be considered.

How Consumers Should Evaluate

For users planning to build a multi-brand smart home system, consider the following:

Verify whether your primary control platform (such as Apple HomePod, Amazon Echo, or Google Nest Hub) has been updated to a firmware version supporting Thread 1.4. Platform firmware updates are typically delivered automatically, but some older devices may not be eligible.
When selecting Thread devices, prioritize products explicitly labeled as Thread 1.4 certified to ensure seamless integration once platforms upgrade. Even if the current platform does not yet support the standard, certified devices are more likely to gain full functionality through future updates.
Understand that during the current transition period, multi-brand Thread devices may still operate in separate sub-networks. This does not affect normal use within a single brand, but cross-brand coordination may be limited. If cross-brand interoperability is a core requirement, consider waiting until platform support is confirmed before large-scale deployment.

Our networking category (25 products) includes devices with various network protocols. Specific protocol versions and compatibility details should be verified on the product detail page. For delivery information, please see our Shipping Policy.

参考来源 / Sources

The Verge, 2026-09-02, Apple Thread 1.4 tvOS 26 Matter Google Amazon

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Matter 1.6 Released: What Changes for Cross-Brand Setup Matter 1.6

On June 17, 2026, the Connectivity Standards Alliance (CSA) officially released the Matter 1.6 specification. This update follows Matter 1.5, which was published in November 2025, and aims to further streamline cross-brand interoperability for smart home devices. For consumers who are building or expanding a smart home system, understanding the differences between Matter versions can inform better purchasing decisions.

Three Key Updates in Matter 1.6

According to the official CSA announcement, Matter 1.6 introduces the following features:

NFC-based end-to-end commissioning: Users can tap their phone against a device to complete network setup, reducing manual steps and simplifying cross-brand pairing. Previously, different brands required distinct setup flows, often forcing users to switch between multiple apps. NFC commissioning aims to unify this experience.
Joint Fabric: Devices from different ecosystems can now operate within a unified network rather than remaining isolated in separate control domains. This means users no longer need to maintain separate control logic for each brand, and multi-brand devices can participate in the same automation scenes.
Thermostat smart suggestions: Context-aware automation recommendations for thermostat devices, enabling a more intelligent balance between energy savings and comfort. This mechanism dynamically adjusts climate strategies based on environmental conditions and user habits rather than relying on fixed schedules.

Matter 1.5 Security Category Support

It is worth noting that Matter 1.5 was the first version to formally support cameras and video door locks. Only devices certified to Matter 1.5 or above can achieve cross-platform interoperability for security products. If a consumer’s primary need is cross-brand security system integration, confirming that a device supports at least Matter 1.5 is essential.

What This Means for Consumers

For consumers selecting smart home devices, the Matter version number directly affects the user experience. If you already own devices from multiple brands, choosing Matter 1.6-compatible products can save significant setup and troubleshooting time. However, the practical availability of Joint Fabric functionality also depends on how quickly platform vendors adopt the update. Consumers should verify whether their primary control platform supports the relevant Matter version before making a purchase.

Our smart locks category (30 products) and smart security category (30 products) include devices with various connectivity protocols. Whether a specific product supports Matter and which version it complies with should be verified on the product detail page. For our return policy, please refer to the Refund and Return Policy.

参考来源 / Sources

CSA Connectivity Standards Alliance, 2026-06-17, Matter 1.6 Enables More Intuitive Setup